Repeated administration of fluvoxamine worsens gentamicin-induced nephrotoxicity in rats

IF 0.7 Q4 PHARMACOLOGY & PHARMACY
Afshin Ramian, I. Javadi, H. Sadeghi, H. Sadeghi, E. Panahi kokhdan, A. Doustimotlagh, R. Abbasi, S. Alizadeh, Hamed Nikbakht
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Abstract

Background: Depression is one of the most prevalent and life-threatening forms of mental disorders in chronic kidney disease. Antidepressant agents such as fluvoxamine are broadly prescribed in this situation. This study investigated the effects of fluvoxamine on gentamicin (GEN)-induced nephrotoxicity in rats. Materials and Methods: Twenty-four male Wistar rats were randomly divided into four groups (n = 6) including (1) control group, (2) GEN group, (3) GEN + fluvoxamine (25 mg/kg) group, and (4) GEN + fluvoxamine (50 mg/kg) group. Fluvoxamine was orally given to animals 45 min before GEN was injected (100 mg/kg, intraperitoneally [i.p.]). Blood urea nitrogen (BUN), creatinine (Cr), sodium (Na+), potassium (K+), and malondialdehyde (MDA) levels in serum were measured. Moreover, the glucose (Glu) and protein (Pro) levels in urine and the ratio of kidney to body weight (g/100g body weight) were determined. Histopathological alterations in kidney were evaluated. Results: GEN significantly increased the Cr and BUN serum levels as well as urine Glu and Pro concentrations (P ≤ 0.001). Fluvoxamine exacerbated the elevation in the indicated parameters. GEN also significantly increased the serum MDA levels. Fluvoxamine had no effect on the elevated serum levels of MDA. GEN did not show any effect on the K+ and Na+ serum concentrations. Increased kidney-to-body weight ratio due to GEN nephrotoxicity was further exacerbated by 25 mg/kg of fluvoxamine (P ≤ 0.001). Pathologic findings also confirm the biochemical results. Conclusion: The data suggest that fluvoxamine worsens the nephrotoxicity of GEN. However, further clinical and animal investigations are required to elucidate the mechanism of this interaction.
反复给药氟伏沙明加重庆大霉素引起的大鼠肾毒性
背景:抑郁症是慢性肾脏疾病中最常见且危及生命的精神障碍之一。抗抑郁剂如氟伏沙明在这种情况下被广泛使用。本研究探讨了氟伏沙明对庆大霉素(GEN)所致大鼠肾毒性的影响。材料与方法:24只雄性Wistar大鼠随机分为4组(n=6),包括(1)对照组,(2)GEN组,(3)GEN+氟伏沙明(25 mg/kg)组和(4)GEN+氟伏沙明(50 mg/kg)组。给动物口服氟伏沙明45 注射GEN前分钟(100 mg/kg,腹膜内[i.p])。测量血清中尿素氮(BUN)、肌酐(Cr)、钠(Na+)、钾(K+)和丙二醛(MDA)水平。此外,还测定了尿液中的葡萄糖(Glu)和蛋白质(Pro)水平以及肾与体重的比值(g/100g体重)。评估肾脏的组织病理学改变。结果:GEN使血清Cr、BUN水平及尿Glu、Pro浓度显著升高(P≤0.001),氟伏沙明加重了指标的升高。GEN也显著提高血清MDA水平。氟伏沙明对血清MDA水平升高没有影响。GEN对K+和Na+血清浓度没有任何影响。由于GEN肾毒性导致的肾与体重比增加进一步加剧了25 mg/kg氟伏沙明(P≤0.001)。病理结果也证实了生化结果。结论:这些数据表明氟伏沙明会加重GEN-的肾毒性。然而,还需要进一步的临床和动物研究来阐明这种相互作用的机制。
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来源期刊
Journal of Reports in Pharmaceutical Sciences
Journal of Reports in Pharmaceutical Sciences Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.40
自引率
0.00%
发文量
0
期刊介绍: The Journal of Reports in Pharmaceutical Sciences(JRPS) is a biannually peer-reviewed multi-disciplinary pharmaceutical publication to serve as a means for scientific information exchange in the international pharmaceutical forum. It accepts novel findings that contribute to advancement of scientific knowledge in pharmaceutical fields that not published or under consideration for publication anywhere else for publication in JRPS as original research article. all aspects of pharmaceutical sciences consist of medicinal chemistry, molecular modeling, drug design, pharmaceutics, biopharmacy, pharmaceutical nanotechnology, pharmacognosy, natural products, pharmaceutical biotechnology, pharmacology, toxicology and clinical pharmacy.
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